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Exact(1)
The research midwife and the trial participant will both be blind to group allocation.
Similar(59)
Staff performing molecular assays was blinded to culture results and both were blinded to epidemiological data.
Both were blinded to the results of the alternative method.
Both were blinded to clinical data, including surgical reports.
Both were blinded to the results of FDG-PET analysis.
Both were blinded to the actual histological diagnosis.
Both were blinded to the patients' smear microscopy test results.
Both were blinded to each subject's group status.
Both were blinded to clinical and demographic patient data.
Both were blinded to the concepts being investigated and one had no medical background.
Both were blinded to the subject condition, and there was a high agreement between them.
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